名稱 | PMP22 Amplification Reference Standard |
型號 | CBP40152 |
報價 | ![]() |
特點(diǎn) | PMP22 Amplification Reference Standard |
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Email: zhangxiangwen@cobioer.com
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基因檢測標(biāo)準(zhǔn)品 > CNV > CBP40152PMP22 Amplification Reference Standard

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PMP22 Amplification Reference Standard
Introduction | ||||
Format | Genomic DNA | |||
Description | This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Studies suggest two alternately used promoters drive tissue-specific expression. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing results in multiple transcript variants. | |||
Technical Data | ||||
Copy number | 3 | |||
Definition | Amplication | |||
Product Information | ||||
Intended Use | Research Use Only | |||
Unit Size | 1ug | |||
Concentration | Download for COA | |||
Purity | Download for COA | |||
DNA electrophoresis | Download for COA | |||
Sanger sequencing | Download for COA | |||
Storage | 4℃ | |||
Expiry | 36 months from the date of manufacture |
PMP22 Amplification Reference Standard